TY - JOUR
T1 - The complete genome sequence of shope (rabbit) fibroma virus
AU - Willer, David O.
AU - McFadden, Grant
AU - Evans, David H.
N1 - Funding Information:
We especially thank Ms. Angela Hollis for performing the hundreds of DNA sequencing reactions upon which this work depended. We also thank J. Barrett, C. Cameron, L. Chen, J. Cao, S. Hota-Mitchell, C. Macaulay, and J. Tyrone for advice, assistance, and commentary on this work during the process of sequence assembly and annotation, and C. Mathews for providing helpful insights into aspects of this work. This study was supported by operating grants awarded to D.E. and G.M. from the Medical Research Council of Canada and to G.M. from the National Cancer Institute of Canada. G.M. is a Medical Research Council of Canada Senior Scientist and D.W. is a recipient of an Ontario Graduate Scholarship in Science and Technology. The College of Biological Sciences DNA sequencing facility at the University of Guelph is partially supported by National Sciences and Engineering Research Council, ORDCF, and CFI funds.
PY - 1999/11/25
Y1 - 1999/11/25
N2 - We have determined the complete DNA sequence of the Leporipoxvirus Shope fibroma virus (SFV). The SFV genome spans 159.8 kb and encodes 165 putative genes of which 13 are duplicated in the 12.4-kb terminal inverted repeats. Although most SFV genes have homologs encoded by other Chordopoxvirinae, the SFV genome lacks a key gene required for the production of extracellular enveloped virus. SFV also encodes only the smaller ribonucleotide reductase subunit and has a limited nucleotide biosynthetic capacity. SFV preserves the Chordopoxvirinae gene order from S012L near the left end of the chromosome through to S142R (homologs of vaccinia F2L and B1R, respectively). The unique right end of SFV appears to be genetically unstable because when the sequence is compared with that of myxoma virus, five myxoma homologs have been deleted (C. Cameron, S. Hota-Mitchell, L. Chen, J. Barrett, J.-X. Cao, C. Macaulay, D. Willer, D. Evans, and G. McFadden, 1999, Virology 264, 298-318). Most other differences between these two Leporipoxviruses are located in the telomeres. Leporipoxviruses encode several genes not found in other poxviruses including four small hydrophobic proteins of unknown function (S023R, S119L, S125R, and S132L), an α 2,3-sialyltransferase (S143R), a protein belonging to the Ig-like protein superfamily (S141 R), and a protein resembling the DNA-binding domain of proteins belonging to the HIN-200 protein family S013L). SFV also encodes a type II DNA photolyase (S127L). Melanoplus sanguinipes entomopoxvirus encodes a similar protein, but SFV is the first mammalian virus potentially capable of photoreactivating ultraviolet DNA damage.
AB - We have determined the complete DNA sequence of the Leporipoxvirus Shope fibroma virus (SFV). The SFV genome spans 159.8 kb and encodes 165 putative genes of which 13 are duplicated in the 12.4-kb terminal inverted repeats. Although most SFV genes have homologs encoded by other Chordopoxvirinae, the SFV genome lacks a key gene required for the production of extracellular enveloped virus. SFV also encodes only the smaller ribonucleotide reductase subunit and has a limited nucleotide biosynthetic capacity. SFV preserves the Chordopoxvirinae gene order from S012L near the left end of the chromosome through to S142R (homologs of vaccinia F2L and B1R, respectively). The unique right end of SFV appears to be genetically unstable because when the sequence is compared with that of myxoma virus, five myxoma homologs have been deleted (C. Cameron, S. Hota-Mitchell, L. Chen, J. Barrett, J.-X. Cao, C. Macaulay, D. Willer, D. Evans, and G. McFadden, 1999, Virology 264, 298-318). Most other differences between these two Leporipoxviruses are located in the telomeres. Leporipoxviruses encode several genes not found in other poxviruses including four small hydrophobic proteins of unknown function (S023R, S119L, S125R, and S132L), an α 2,3-sialyltransferase (S143R), a protein belonging to the Ig-like protein superfamily (S141 R), and a protein resembling the DNA-binding domain of proteins belonging to the HIN-200 protein family S013L). SFV also encodes a type II DNA photolyase (S127L). Melanoplus sanguinipes entomopoxvirus encodes a similar protein, but SFV is the first mammalian virus potentially capable of photoreactivating ultraviolet DNA damage.
UR - http://www.scopus.com/inward/record.url?scp=0033604621&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033604621&partnerID=8YFLogxK
U2 - 10.1006/viro.1999.0002
DO - 10.1006/viro.1999.0002
M3 - Article
C2 - 10562495
AN - SCOPUS:0033604621
SN - 0042-6822
VL - 264
SP - 319
EP - 343
JO - Virology
JF - Virology
IS - 2
ER -